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有证据表明,在C/D盒小核仁核糖核蛋白(snoRNP)生物合成过程中,AAA+蛋白TIP48和TIP49在15.5K与相关的NOP56和NOP58蛋白之间建立了相互作用。

Evidence that the AAA+ proteins TIP48 and TIP49 bridge interactions between 15.5K and the related NOP56 and NOP58 proteins during box C/D snoRNP biogenesis.

作者信息

McKeegan Kenneth Scott, Debieux Charles Maurice, Watkins Nicholas James

机构信息

RNA Biology Group, ICaMB, University of Newcastle upon Tyne, Newcastle upon Tyne, UK.

出版信息

Mol Cell Biol. 2009 Sep;29(18):4971-81. doi: 10.1128/MCB.00752-09. Epub 2009 Jul 20.

Abstract

The box C/D small nucleolar RNPs (snoRNPs) are essential for the processing and modification of rRNA. TIP48 and TIP49 are two related AAA(+) proteins that are essential for the formation of box C/D snoRNPs. These proteins are key components of the pre-snoRNP complexes, but their exact role in box C/D snoRNP biogenesis is largely uncharacterized. Here we report that TIP48 and TIP49 interact with one another in vitro, and only the TIP48/TIP49 complex, but not the individual proteins, possesses significant ATPase activity. Loss of TIP48 and TIP49 results in a change in pre-snoRNA levels and a loss of U3 snoRNA signal in the Cajal body. We show that TIP48 and TIP49 make multiple interactions with core snoRNP proteins and biogenesis factors and that these interactions are often regulated by the presence of ATP. Furthermore, we demonstrate that TIP48 and TIP49 efficiently bridge interactions between the core box C/D proteins NOP56 or NOP58 and 15.5K. Our data imply that the snoRNP assembly factor NUFIP can regulate the interactions between TIP48 and TIP49 and the core box C/D proteins. We suggest that snoRNP assembly involves an intricate series of interactions that are mediated/regulated by bridging factors and chaperones.

摘要

C/D盒小核仁核糖核蛋白颗粒(snoRNP)对于核糖体RNA(rRNA)的加工和修饰至关重要。TIP48和TIP49是两种相关的AAA(+)蛋白,对于C/D盒snoRNP的形成必不可少。这些蛋白是前体snoRNP复合物的关键组分,但它们在C/D盒snoRNP生物发生中的具体作用很大程度上尚不明确。在此我们报告,TIP48和TIP49在体外相互作用,并且只有TIP48/TIP49复合物而非单个蛋白具有显著的ATP酶活性。TIP48和TIP49的缺失导致前体snoRNA水平的改变以及卡哈尔体中U3 snoRNA信号的丧失。我们表明,TIP48和TIP49与核心snoRNP蛋白及生物发生因子发生多种相互作用,并且这些相互作用常常受ATP存在的调节。此外,我们证明TIP48和TIP49有效地介导了核心C/D盒蛋白NOP56或NOP58与15.5K之间的相互作用。我们的数据表明,snoRNP组装因子NUFIP可以调节TIP48和TIP49与核心C/D盒蛋白之间的相互作用。我们认为,snoRNP组装涉及由桥接因子和分子伴侣介导/调节的一系列复杂的相互作用。

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